Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0001361
Disease: Acute tonsillitis
Acute tonsillitis 		0 1 0 0 1 1.7E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.7E-03
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		0 31 0 0 1 1.6E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.7E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 3.3E-03
CUI: C0854467
Disease: Myelosuppression
Myelosuppression 		0 1 0 0 1 1.7E-03
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess 		0 3 0 0 2 3.3E-03
CUI: C1833450
Disease: HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO 		0 1 0 0 1 1.7E-03
CUI: C1837991
Disease: Colorectal Adenomatous Polyposis, Autosomal Recessive
Colorectal Adenomatous Polyposis, Autosomal Recessive 		0 112 0 0 2 2.8E-03
CUI: C1857845
Disease: CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding) 		0 1 0 0 1 1.7E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.6E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.7E-03
CUI: C4016911
Disease: FAMILIAL ADENOMATOUS POLYPOSIS 2 WITH PILOMATRICOMAS
FAMILIAL ADENOMATOUS POLYPOSIS 2 WITH PILOMATRICOMAS 		0 1 0 0 1 1.7E-03
CUI: C0338502
Disease: Hypoplasia of the optic nerve
Hypoplasia of the optic nerve 		59 0 1 6.1E-04 0 0
CUI: C1855483
Disease: Progressive spastic paraplegia
Progressive spastic paraplegia 		59 0 1 6.1E-04 0 0
CUI: C1857704
Disease: Abnormal myelination
Abnormal myelination 		49 0 1 6.2E-04 0 0
CUI: C1865037
Disease: Cone-shaped epiphysis
Cone-shaped epiphysis 		49 0 1 6.2E-04 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 1 6.2E-04 0 0
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		45 0 1 6.2E-04 0 0
CUI: C1849488
Disease: Increased serum pyruvate
Increased serum pyruvate 		45 0 1 6.2E-04 0 0
CUI: C0240421
Disease: Progressive muscle weakness
Progressive muscle weakness 		44 0 1 6.2E-04 0 0
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		42 0 1 6.2E-04 0 0
CUI: C0234860
Disease: Weak cry
Weak cry 		42 0 1 6.2E-04 0 0
CUI: C1853235
Disease: Sclerocornea
Sclerocornea 		42 0 1 6.2E-04 0 0
CUI: C1854912
Disease: Short long bone
Short long bone 		42 0 1 6.2E-04 0 0